This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human VEGFR-2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Human VEGFR-2 are added to the micro ELISA plate wells. Human VEGFR-2 in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Human VEGFR-2.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human VEGFR-2. The concentration of Human VEGFR-2 in the samples is then determined by comparing the OD of the samples to the standard curve.
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human VWF. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Human VWF are added to the micro ELISA plate wells. Human VWF in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Human VWF.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human VWF. The concentration of Human VWF in the samples is then determined by comparing the OD of the samples to the standard curve.
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human αFP. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Human αFP are added to the micro ELISA plate wells. Human αFP in samples (or standards) combines with the coated antibody and HRP linked detection antibody special to Human αFP.Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The OD value is proportional to the concentration of Human αFP. The concentration of Human αFP in the samples is then determined by comparing the OD of the samples to the standard curve.
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Monkey Cortisol. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Monkey Cortisol are added to the micro ELISA plate wells. Monkey Cortisol in samples (or standards) competes with a fixed amount of Cortisol on the solid phase supporter for sites on the HRP linked detection antibody specific to Cortisol. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Monkey Cortisol in the samples is then determined by comparing the OD of the samples to the standard curve.
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Monkey E2. Samples (or Standards) and Horseradish Peroxidase (HRP) linked antibody specific for Monkey E2 are added to the micro ELISA plate wells. Monkey E2 in samples (or standards) competes with a fixed amount of E2 on the solid phase supporter for sites on the HRP linked detection antibody specific to E2. Excess conjugate and unbound sample or standard are washed from the plate. The substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450±2 nm. The concentration of Monkey E2 in the samples is then determined by comparing the OD of the samples to the standard curve.
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